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3-(5-Methylfuran-2-yl)propanoic acid is a synthetic, non-proteinogenic amino acid characterized by a standard three-carbon propanoic acid backbone with an amino functional group (-NH2) located at the alpha-carbon (C2) and a distinctive 5-methylfuran-2-yl substituent at the beta-carbon (C3), where the furan ring—a five-membered aromatic heterocycle containing an oxygen atom—provides its unique structural and electronic properties, distinguishing it from canonical amino acids.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $195 | - | In Stock | |
| 5 mg | $483 | - | In Stock | |
| 10 mg | $691 | - | In Stock | |
| 25 mg | $1,080 | - | In Stock |
| Description | 3-(5-Methylfuran-2-yl)propanoic acid is a synthetic, non-proteinogenic amino acid characterized by a standard three-carbon propanoic acid backbone with an amino functional group (-NH2) located at the alpha-carbon (C2) and a distinctive 5-methylfuran-2-yl substituent at the beta-carbon (C3), where the furan ring—a five-membered aromatic heterocycle containing an oxygen atom—provides its unique structural and electronic properties, distinguishing it from canonical amino acids. |
| Synonyms | 3-(5-Methyl-furan-2-yl)-propionic acid |
| Molecular Weight | 154.16 |
| Formula | C8H10O3 |
| Cas No. | 1456-08-2 |
| Smiles | O=C(O)CCC=1OC(=CC1)C |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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